Aim/purpose: Fibroblast activation protein-(FAP)-ligands, a novel class of tracers for PET/CT imaging, demonstrated promising results in previous studies in various malignancies compared to standard [F]FDG PET/CT. Ga-labeled fibroblast activation protein inhibitor-([Ga]Ga-DOTA-FAPI)-PET/CT impresses with sharp contrasts in terms of high tumor uptake and low background noise leading to clear delineation. [F]FDG PET/CT has limited accuracy in bladder cancer due to high background signal. Therefore, we sought to evaluate the diagnostic potential of [Ga]FAPI in patients with bladder cancer.
Material And Methods: This retrospective analysis consisted of 8 patients (median age 66), 7 of whom underwent both [Ga]FAPI and [F]FDG PET/CT scans with a median time interval of 5 days (range 1-20 days). Quantification of tracer uptake was determined with SUV and SUV. Furthermore, the tumor-to-background ratio (TBR) was derived by dividing the SUV of tumor lesions by the SUV of adipose tissue, skeletal muscle, and blood pool.
Results: Overall, 31 metastases were detected in five patients including lymph node metastases (n = 23), bone metastases (n = 4), lung metastases (n = 3), and a peritoneal metastasis (n = 1). In one patient, [Ga]FAPI demonstrated significant uptake in the primary tumor located in the bladder wall. [Ga]FAPI-PET/CT demonstrated significantly higher uptake compared to [F]FDG PET/CT with higher mean SUV (8.2 vs. 4.6; p = 0.01). Furthermore, [Ga]FAPI detected additional 30% (n = 9) lesions, missed by [F]FDG. TBR demonstrated favorable uptake for [Ga]FAPI in comparison to [F]FDG. Significant differences were determined with regard to metastasis/blood pool ([Ga]FAPI 5.3 vs [F]FDG 1.9; p = 0.001).
Conclusion: [Ga]FAPI-PET/CT is a promising diagnostic radioligand for patients with bladder cancer. This first described analysis of FAP-ligand in bladder cancer revealed superiority over [F]FDG in a small patient cohort. Thus, this so far assumed potential has to be confirmed and extended by larger and prospective studies.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9296390 | PMC |
http://dx.doi.org/10.1007/s11307-022-01715-3 | DOI Listing |
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